Regulatory affairs courses, webinars, conferences and meetings

We offer a comprehensive programme of training courses, conferences, meetings and webinars on a wide range of regulatory affairs topics.

Our courses are delivered by highly regarded experts from industry and government agencies and are suitable for professionals at all stages of their regulatory career. Read more about the different regulatory affairs course categories and how these relate to your own career.

Our commitment to quality

TOPRA is proud to have provided gold standard training for regulatory affairs professionals for more than 40 years. Our commitment to the profession, to everyone who attends our training and to employers who entrust their staff development to us, is given in our Quality Statement.

Start dateTitleDescriptionCityCountry
22/10/2024Health Economics From a Regulatory PerspectiveHealth economics and Health Technology Assessment (HTA) during the development of a new drug are becoming increasingly important. If a drug is to reach the patient after regulatory approval, it must undergo a health economic evaluation, a basis for pricing and decisions on subsidies. This takes place at national level in the various EU countries. Hear from TLV and Industry about the new EU HTA Regulation (EU) 2021/2282 (HTAR) which will be applied from January 2025 for certain medicines, Joint Clinical Assessment (JCA) and HTA strategy during drug development. This evening is an excellent opportunity to hear the latest in this field. You also get the opportunity to meet colleagues in a relaxed and sociable setting.UppsalaSwedenSWEOCT24
23/10/2024Post-Market Surveillance and Vigilance for Medical DevicesThis Masterclass is also Module 16 of the MSc Regulatory Affairs and will help to define the terminology and explain the concepts of vigilance and post-market surveillance, their practical applications and integration into the life cycle of a medical device. This course will focus on meeting European requirements.LondonUnited KingdomMSCMD16F
23/10/2024Post-Market Surveillance and Vigilance for Medical DevicesThis Masterclass is also Module 16 of the MSc Regulatory Affairs and will help to define the terminology and explain the concepts of vigilance and post-market surveillance, their practical applications and integration into the life cycle of a medical device. This course will focus on meeting European requirements.Online MSCMD16O
29/10/2024Sponsored Webinar: Regulatory Strategies in the ME RegionFREE SPONSORED WEBINAR - Gain insights into the MENA pharmaceutical market. This session will cover regulatory frameworks, effective business strategies, and intellectual property protection, providing you with the tools to navigate and thrive in this dynamic region. OnlineSPWB2PI24
29/10/2024Navigating Regulatory Changes in Moldova and UkraineJoin this webinar to explore regulatory strategies in Moldova and Ukraine during this complex period and the roadmap to integration with the EU. OnlineMDUAOCT24
31/10/2024Biotech, Cell & Gene Therapies: Risk Based Approach To ATMPsFollowing on from the successful series of webinars on ATMPs in 2021, Dr Bridget Heelan returns with an updated presentation on the risk based approach to ATMPs. OnlineBIOOCT24
06/11/2024CRED Prescription to Non-Prescription Medicines Switch in EUThe course will provide a comprehensive overview of the regulatory framework on Rx to OTC switch in Europe and the specificities of non-prescription medicines. It will also provide a number of examples and concrete cases to help understanding and turning theory into practice.Online CREDPNP24
12/11/2024Overview of EU Pharmaceutical Regulatory AffairsModule 0 of the MSc: This course covers all aspects of the product development process, and provides a sound overview of EU legislation and regulatory procedures, including the central role regulatory affairs plays in modern healthcare companies.LisbonPortugalIC22024
14/11/2024Sponsored Webinar: What to know about FDA diversity plan?FREE SPONSORED WEBINAR - Gain a comprehensive understanding of the new US Diversity Plan Guidance and its implications for the pharmaceutical and biotech industry. OnlineSPWFORT24
19/11/2024CRED IVD Regulatory Affairs for Global MarketsIncrease your impact as a regulatory professional and expand your IVD expertise beyond Europe with this two and a half day course.LondonUnited KingdomIVDGM24
19/11/2024CRED IVD Regulatory Affairs for Global MarketsIncrease your impact as a regulatory professional and expand your IVD expertise beyond Europe with this two and a half day course.Online IVDGON24
19/11/2024Regulatory Strategy for a NAS: Global Clinical DevelopmentRegulatory Strategy for a New Active Substance: Global Clinical Development  is also Module 4 of the MSc and will help you to understand and develop regulatory strategies for all aspects of global clinical research, as well as address practical regulatory issues in this area.BerlinGermanyMSCM42024
19/11/2024Regulatory Strategy for a NAS: Global Clinical DevelopmentRegulatory Strategy for a New Active Substance: Global Clinical Development  is also Module 4 of the MSc and will help you to understand and develop regulatory strategies for all aspects of global clinical research, as well as address practical regulatory issues in this area.Online MSCM42024O
20/11/2024Clinical Trials with Drugs, Medical Devices and ATMPClinical trials in Europe follow different rules and regulations, CTR, MDR, IVDR and combined studies have their challenges. We hear about COMBINE, experiences with clinical trials of drugs, medical devices, combination products, ATMP (cell and gene therapies) and some news about TOPRA. You get the opportunity to meet colleagues in a relaxed and pleasant environment. The meeting is open to anyone who works with and is interested in regulatory affairs.MölndalSwedenSWENOV24
22/11/2024UK Regulatory of SaMD and AlaMD - Evolution and OutlookThe pace of developments in the software and AI landscape and the commensurate risks and opportunities posed by healthcare technologies pose an important challenge for regulators.  This webinar will review the evolution of UK policy and guidance on Software as a Medical Device and AI as a Medical Device and provide an outlook on upcoming developments.ONLINEUnited KingdomSAMDANOV24
26/11/2024CRED Optimising Regulatory Strategies for Orphan DrugsThere are regulatory processes and procedures to expedite approval and access, and to help support the development of medicines for the treatment of rare diseases. This course will provide key information about those regulatory processes and first-hand insights on how to get the best out of them.Online OD24
28/11/2024TOPRA Awards for Regulatory Excellence 2024Join us at Chartered Accountants Hall in London on 28 November for the TOPRA Awards for Regulatory Excellence to celebrate the achievements of individuals, teams and organisations in the global regulatory affairs community.LondonUnited KingdomAWARDS2024
28/11/2024CRED Regulatory Update: Veterinary Variations in the EUThis is a comprehensive overview of how to prepare and submit variations to VMP marketing authorisations. It provides an update on the latest changes and advice on best practice for experienced regulatory professionals. OnlineVETTEST24
29/11/2024Essentials of European Medical Device Regulatory AffairsThis course will provide an overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment.BerlinGermanyMDBAS1124
29/11/2024Essentials of European Medical Device Regulatory AffairsThis course will provide an overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment.Online MDBAS1124O
04/12/2024Regulatory Strategy in the Post Market PhaseThis Masterclass is also Module 17 of the MSc Regulatory Affairs (previously know as Regulatory and Related Activities Through the Device Lifecycle) will provide regulatory affairs professionals with insight into the strategic issues affecting the commercial and regulatory maintenance of a medical device throughout its lifecycle, with focus on post-launch activities and future pressures.LondonUnited KingdomMD172024
04/12/2024Regulatory Strategy in the Post Market PhaseThis Masterclass is also Module 17 of the MSc Regulatory Affairs (Previously titled Regulatory & Related Activities Through the Device) and will provide regulatory affairs professionals with insight into the strategic issues affecting the commercial and regulatory maintenance of a medical device throughout its lifecycle, with focus on post-launch activities and future pressures.Online MD172024O
10/12/2024EU AI Act Implementation for Medical DevicesAn overview of the impact of the EU AI Act for medical devices, key milestones and practical recommendation for compliance by medical device manufacturers.OnlineUnited KingdomSAMDDEC24
28/03/2025Regulatory Careers Live 2025 - Dublin, IrelandRegulatory Careers Live is Europe’s only careers fair dedicated to healthcare regulatory affairs. It is free to attend and your opportunity to meet with potential future employers and get essential advice from some of the most respected and influential leaders in the field of regulatory affairs.DublinIrelandRCLIE25
13/06/2025Regulatory Careers Live 2025 - Brussels, Belgium - In-PersonRegulatory Careers Live is Europe’s only careers fair dedicated to healthcare regulatory affairs. It is free to attend and your opportunity to meet with potential future employers and get essential advice from some of the most respected and influential leaders in the field of regulatory affairs.BrusselsUnited KingdomRCL25BRU
09/09/2025Regulatory Careers Live 2025 - London, United KingdomRegulatory Careers Live is Europe’s only careers fair dedicated to healthcare regulatory affairs. It is free to attend and your opportunity to meet with potential future employers and get essential advice from some of the most respected and influential leaders in the field of regulatory affairs.LondonUnited KingdomRCL25LON
29/09/2025TOPRA Symposium 2025 Exhibitor Package - OFFERA truly unique and valuable event in regulatory affairs – the only conference entirely focused on healthcare regulatory affairs allowing you to meet a closely defined group of professionalsBerlinGermanySYM2025EXH